Identification of Active Edge Sites for Electrochemical H 2 Evolution from MoS 2 Nanocatalysts
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Materials and methods are available as supporting material on Science Online.
The cell specifically designed for studies on UHV-transferred samples is sealed upon the imaged (111) face of the sample with a viton o-ring exposing ∼0.10 cm 2 to the H 2 SO 4 electrolyte (pH 0.24 23°C) and cyclic voltammograms are recorded. This procedure ensures a one-to-one correlation between the imaged MoS 2 nanoparticles and the measured activity for hydrogen evolution.
We note that Au atoms along the particle edge also scale with the edge length; however previous experimental and computational studies have shown negligible interaction between the MoS 2 and the support ( 14 15 ) leading us to conclude that such sites would be as inactive as those of the blank samples prepared without MoS 2 deposition.
In our comparison with Pt(111) we assumed that the observed HER on this surface is dominated by terrace atoms not defects. This is the consensus in the literature ( 7 ).
This project was supported by the Danish Strategic Research Council. T.F.J. acknowledges an H. C. Ørsted Postdoctoral Fellowship from the Technical University of Denmark. The Center for Individual Nanoparticle Functionality is supported by the Danish National Research Foundation. The Center for Atomic-scale Materials Design is supported by the Lundbeck Foundation.
